FDA Device recall Z-0238-2018
UniCel DxH Slidemaker Stainer, Part Number 75222, for use with automated hematology analyzer
- FDA Device
- Class II
- terminated
- Published 2017-12-20
On 2017-12-20 the FDA classified a Class II recall of UniCel DxH Slidemaker Stainer, Part Number 75222, for use with automated hematology analyzer by Beckman Coulter, citing the shield for the Single-Tube Station on the DxH instrument may interfere with sample aspiration in the open vial position.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0238-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-11-03 |
| Published | 2017-12-20 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Beckman Coulter |
| Distribution | AR, CA, HI, MD, OH, WA |
Product
UniCel DxH Slidemaker Stainer, Part Number 75222, for use with automated hematology analyzer
Reason
The shield for the Single-Tube Station on the DxH instrument may interfere with sample aspiration in the open vial position.
Identifiers
| code_info | Serial Numbers: AW09034, AV40142, AU19113 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0238-2018%22
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